FDA NDC Directory · JSON-LD · Markdown

Doxepin

NDC 27241-280 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAjanta Pharma USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218564
Dosage form / routeTABLET · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (3 mg/1)
Marketing started20240701
Package count1

External sources

Source: openFDA. Public-domain (CC0).